Canonical Allele Identifier: PA658680999
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455205
ClinVar RCV Id: RCV000554932 RCV000765688 RCV002431517 RCV003493624
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Asp839His
CA346754328
NM_000179.3:c.2515G>C